2-Amino-5-chlorobenzophenone → HCID 15125288, compound

HRID 1497039Notes

Reaction equation

[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=O.[CH:17]([C:20](=O)[CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23])([CH3:19])[CH3:18]>>[CH2:25]([O:24][C:22]([C:21]1[C:20]([CH:17]([CH3:19])[CH3:18])=[N:1][C:2]2[C:3]([C:9]=1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[CH:4][C:5]([Cl:8])=[CH:6][CH:7]=2)=[O:23])[CH3:26]

Participants

Reactant 2

HCID 128702-Amino-5-chlorobenzophenone

HCID 81583Ethyl isobutyrylacetate

Product 1

HCID 15125288HCID 15125288, compound

Procedure

The title compound was prepared in analogy to example 1 step A using (2-amino-5-chlorophenyl)(phenyl)methanone and ethyl 3-isopropyl-3-oxopropanoate as starting materials.

Sources & evidence

ORD record: ord-202659b063bf45d38f1afcd3a83a23a2
Source dataset: uspto-grants-2015_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09199938B2

Reaction notes

Loading…